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Granulomatosis With Polyangiitis Presenting as Chest Pain: A Case Report
Kindalem Fentie1, Swathi Singanamala2, Omar Hozayen1
1Medicine, Trinity Medical Sciences University, Warner Robins, USA.
Abstract:
Granulomatosis with polyangiitis (GPA) is a relatively rare systemic autoimmune disorder of small and medium size blood vessels affecting multiple organs with a wide range of clinical presentations. We present a 57-year-old Caucasian male who presented to the ER with midsternal chest pain. He was hospitalized for non-ST elevated myocardial infarction (NSTEMI) and later diagnosed with pauci-immune necrotizing crescentic glomerulonephritis confirmed with renal biopsy.
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